Linked Data
ClinVar Variation Id:
334576
dbSNP Id:
rs374191606
gnomAD v2:
2-225335297-A-T
gnomAD v3:
2-224470580-A-T
gnomAD v4:
2-224470580-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.224470580A>T , CM000664.2:g.224470580A>T | GRCh38 |
| NC_000002.11:g.225335297A>T , CM000664.1:g.225335297A>T | GRCh37 |
| NC_000002.10:g.225043541A>T | NCBI36 |
| NG_032169.1:g.119818T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264414.9:c.*3665T>A MANE Select | ENSP00000264414.4:n.*3665T>A | |
| ENST00000264414.8:c.*3665T>A | ENSP00000264414.4:n.*3665T>A | |
| ENST00000344951.8:c.*3665T>A | ENSP00000343601.4:n.*3665T>A | |
| NM_001257197.1:c.*3665T>A | NP_001244126.1:n.*3665T>A | |
| NM_001257198.1:c.*3665T>A | NP_001244127.1:n.*3665T>A | |
| NM_003590.4:c.*3665T>A | NP_003581.1:n.*3665T>A | |
| NM_003590.5:c.*3665T>A MANE Select | NP_003581.1:n.*3665T>A | |
| NM_001257198.2:c.*3665T>A | NP_001244127.1:n.*3665T>A | |
| NM_001257197.2:c.*3665T>A | NP_001244126.1:n.*3665T>A |